The present invention relates to novel oxazolidinones (Formula I): or a pharmaceutically acceptable salt having ring A characterized by N-containing monocyclic, bicyclic or spirocyclic substituents, to their preparation, and to their use as drugs for treating Mycobacterium tuberculosis and other microbial infections, either alone or in combination with other anti-infective treatments.
本发明涉及新型
噁唑烷酮(
化学式I):或具有由含氮的单环、双环或螺环取代基特征的环A的药用盐,以及其制备方法,以及作为用于治疗结核分枝杆菌和其他微
生物感染的药物的用途,可以单独使用或与其他抗感染治疗结合使用。